A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567386



Internal ID20940457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45385779..45386311hg38UCSC Ensembl
chr6:45353516..45354048hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271391
Samples
Known GenesRUNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer